US2023405881A1PendingUtilityA1

3d printing and fabrication

Assignee: UNIV KING ABDULLAH SCI & TECHPriority: Jun 21, 2022Filed: Jun 16, 2023Published: Dec 21, 2023
Est. expiryJun 21, 2042(~15.9 yrs left)· nominal 20-yr term from priority
B29C 33/3892B33Y 30/00B33Y 80/00B29C 71/04B33Y 10/00B29C 64/118B29L 2031/00B29K 2067/046B33Y 70/10B33Y 70/00B29C 2071/0045B29C 2035/0827
49
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Claims

Abstract

A modified approach for coral restoration by merging 3D printing and molding techniques is presented. This is achieved by 3D scanning live coral specimens, retrieved from sea dives, to obtain a CAD model of the complete coral 3D construction with complex geometries. Select areas of the model are flattened to create a 2D base for micro-fragment adhesion. From the CAD models, disclosed embodiments propose two methods of fabrication. Method A consists of 3D printing the CAD models with commercial thermoplastic materials to create a negative mold, subsequently loaded with synthesized Calcium Carbonate Photoinitiated (CCP) ink to form an eco-friendly coral skeleton. Method B uses syringe-based extrusion 3D printing to directly print a coral skeleton with CCP ink. Both methods are evaluated as a combined proof-of-concept process, 3D CoraPrint, for coral gardening and restoration and providing details required for mimicking coral and bone 3D structures for implantation in bone grafting applications.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . An apparatus for a subject comprising: a fabrication of a digital scan of the subject and having a seeded micro-fragment of the subject attached thereto. 
     
     
         2 . The apparatus of  claim 1 , wherein the fabrication is 3D printed. 
     
     
         3 . The apparatus of  claim 2 , wherein the 3D printed fabrication comprises a thermoplastic filament. 
     
     
         4 . The apparatus of  claim 1 , wherein the fabrication is molded. 
     
     
         5 . The apparatus of  claim 1 , wherein the subject is a clonal organism. 
     
     
         6 . The apparatus of  claim 5 , wherein the clonal organism is a marine invertebrate. 
     
     
         7 . The apparatus of  claim 6 , wherein the marine invertebrate is a coral. 
     
     
         8 . The apparatus of  claim 7 , wherein the coral is selected from the group consisting of  Acroporidae, Acropora,  and  Acropora hemprichh.    
     
     
         9 . The apparatus of  claim 1 , wherein the subject is selected from the group consisting of a human, a mammal, a reptile, a bird, a fish, an amphibian, and an invertebrate. 
     
     
         10 . The apparatus of  claim 1 , wherein the fabrication is cured under UV or visible light. 
     
     
         11 . A method of manufacturing a scaffold for a subject comprising:
 scanning the subject to form a digital model of the subject;   modifying a digital geometry of the digital model to form a modified digital model;   fabricating the modified digital model to form a scaffold; and   seeding a micro-fragment of the subject to the scaffold.   
     
     
         12 . The method of  claim 11 , wherein the scaffold is cured under UV or visible light. 
     
     
         13 . The method of  claim 11 , wherein the modifying step comprises selecting an area of the digital model to be flattened to form the modified digital model and wherein the modified digital model is a two dimensional (2D) base for micro-fragment adhesion. 
     
     
         14 . The method of  claim 11 , wherein the fabrication step comprises a 3D printing with a thermoplastic filament to form a mold and filling the mold with an ink. 
     
     
         15 . The method of  claim 14 , wherein the 3D printing is submerged with the thermoplastic filament in a liquid silicon. 
     
     
         16 . The method of  claim 14 , wherein the thermoplastic filament comprises a polylactic acid (PLA). 
     
     
         17 . The method of  claim 11 , wherein the fabrication step comprises a direct 3D printing with a syringe-based Fused Deposition Modeling (FDM) and an ink. 
     
     
         18 . The method of  claim 11 , wherein the seeding step comprises adding cells on the scaffold to produce surfaces for bone grafting. 
     
     
         19 . The method of  claim 14 , wherein the ink is a calcium carbonate photoinitiated (CCP) ink. 
     
     
         20 . The method of  claim 19 , wherein the CCP ink comprises a calcium carbonate and a resin. 
     
     
         21 . The method of  claim 20 , wherein the calcium carbonate:resin has an average ratio of 9:1 to 1:1. 
     
     
         22 . The method of  claim 20 , wherein the calcium carbonate:resin has an average ratio of 7:3. 
     
     
         23 . The method of  claim 20 , wherein a constitution of the CCP ink consists of 20-75% resin. 
     
     
         24 . The method of  claim 23 , wherein the calcium carbonate is in a range of approximately to the resin. 
     
     
         25 . The method of  claim 20 , wherein the constitution of CCP ink comprises minerals. 
     
     
         26 . The method of  claim 25 , wherein the minerals are selected from the group consisting of magnesium, zinc, and iron oxide. 
     
     
         27 . The method of  claim 14 , wherein the ink is a calcium phosphate paste (CPP). 
     
     
         28 . The method of  claim 27 , wherein a constitution of the CPP consists of 20-75% resin. 
     
     
         29 . The method of  claim 28 , wherein the calcium phosphate is in a range of approximately 10-75% to the resin. 
     
     
         30 . The method of  claim 27 , wherein the constitution of CPP comprises minerals. 
     
     
         31 . The method of  claim 30 , wherein the minerals are selected from the group consisting of magnesium, zinc, and iron oxide. 
     
     
         32 . The method of  claim 11 , wherein the subject is a clonal organism. 
     
     
         33 . The method of  claim 32 , wherein the clonal organism is a marine invertebrate. 
     
     
         34 . The method of  claim 33 , wherein the marine invertebrate is a coral. 
     
     
         35 . The method of  claim 34 , wherein the coral is selected from the group consisting of  Acroporidae, Acropora,  and  Acropora hempricha.    
     
     
         36 . The method of  claim 11 , wherein the subject is selected from the group consisting of a human, a mammal, a reptile, a bird, a fish, an amphibian, and an invertebrate. 
     
     
         37 . The method of  claim 14 , wherein the mold is recyclable at least 10 times.

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